Evidence map›Paper›PMID 37894350›Full record

ArticleCancers2023

Insulin-like Growth Factor II mRNA-Binding Protein 1 Regulates Pancreatic Cancer Cell Growth through the Surveillance of

Davide Di Fusco, Maria Teresa Segreto, Giulia Di Maggio, Andrea Iannucci, Claudia Maresca, Antonio Di Grazia, Marco Colella, Carmine Stolfi, Giovanni Monteleone, Ivan Monteleone

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 32% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Davide Di FuscoDepartment of Systems Medicine, University of "Tor Vergata", 00133 Rome, Italy.ORCID 0000-0002-8908-9237
Maria Teresa SegretoDepartment of Systems Medicine, University of "Tor Vergata", 00133 Rome, Italy.
Giulia Di MaggioDepartment of Systems Medicine, University of "Tor Vergata", 00133 Rome, Italy.ORCID 0000-0002-1214-5843
Andrea IannucciDepartment of Biomedicine and Prevention, University of "Tor Vergata", 00133 Rome, Italy.ORCID 0000-0001-5194-8959
Claudia MarescaDepartment of Systems Medicine, University of "Tor Vergata", 00133 Rome, Italy.
Antonio Di GraziaDepartment of Systems Medicine, University of "Tor Vergata", 00133 Rome, Italy.
Marco ColellaDepartment of Systems Medicine, University of "Tor Vergata", 00133 Rome, Italy.
Carmine StolfiDepartment of Systems Medicine, University of "Tor Vergata", 00133 Rome, Italy.ORCID 0000-0002-6354-2443
Giovanni MonteleoneDepartment of Systems Medicine, University of "Tor Vergata", 00133 Rome, Italy.ORCID 0000-0003-1339-9076
Ivan MonteleoneDepartment of Biomedicine and Prevention, University of "Tor Vergata", 00133 Rome, Italy.ORCID 0000-0002-3212-832X
University of Rome Tor Vergata · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A number of data indicate that the sources of different kinds of PDAC may be discovered at the transcription/transduction stage. RNA metabolism is manipulated at various steps by different RNA-binding proteins (RBPs), and the deregulation or irregular activity of RBPs is known to contribute to tumor promotion and progression. The insulin-like growth factor 2 mRNA-binding protein family (IMPs), and IMP1 in particular, has been linked with a poor prognosis in PDAC patients; however, little is known about its contribution in PDAC carcinogenesis. In this study, we investigated the function of IMP1 in PDAC. To evaluate IMP1 expression and correlation with PDAC prognosis, we utilized several public databases. Using a specific siRNA IMP1, we analyzed cell death and cell cycle progression in PDAC cell lines and 3D spheroids. The role of IMP1 was also evaluated in vivo in a Panc-1-derived tumor xenograft murine model. Public data suggest that PDAC patients with higher expression of IMP1 showed poor overall and progression-free survival. IMP1 silencing leads to reduced cell growth in PDAC cells and three-dimensional spheroids. Abrogation of IMP1 in PDAC cells showed lower levels of

Indexed as

CDC25ACDK2cell cyclecell deathIGF2BP1IMP1pancreatic cancerPDACRBPRNA-binding protein

Identifiers

PMID37894350
PMCPMC10605367
OpenAlexW4387642631

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.